# FDA recall Z-1749-2022

> **FUJIFILM Healthcare Americas Corporation** · Class II · device recall initiated 2022-07-12.

## Product

Surpria: Software Version V3.11, V3.22

## Reason for recall

Error 00003050 or 00003052  may occur during scanning, the captured images will not be reconstructed and the Raw Data will not be displayed in the work list.result, may result in the need for additional scanning to capture the images properly for reconstruction, thereby exposing the patient to additional radiation

## Distribution

US Nationwide Distribution

## Key facts

- **Recall number:** Z-1749-2022
- **Recalling firm:** FUJIFILM Healthcare Americas Corporation
- **Classification:** Class II
- **Product type:** device
- **Status:** Ongoing
- **Initiation date:** 2022-07-12
- **Report date:** 2022-09-21

- **Voluntary/Mandated:** Voluntary: Firm initiated
- **Location:** Lexington, MA, United States

## Primary source

FDA Enforcement Reports: https://www.accessdata.fda.gov/scripts/ires/index.cfm?Product=Z-1749-2022

## Citation

> AI Analytics. FDA recall Z-1749-2022. Retrieved 2026-06-09 from https://api.ai-analytics.org/recall/Z-1749-2022. Source: US FDA. Licensed CC0.

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